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1 ative SDK channels, and nitrergic inhibitory junction potentials.
2 eased the amplitude of purinergic excitatory junction potentials.
3 cation of longitudinal stretch inhibited all junction potentials.
4 he amplitude of slow waves and of inhibitory junction potentials.
5 microM) affected the amplitude of excitatory junction potentials (2 +/- 5 % and -3 +/- 10 %) or NCTs
6                                   Inhibitory junction potentials and responses to exogenous beta-NAD,
7 e, and cyclopiazonic acid, reduce inhibitory junction potentials and responses to sodium nitroprussid
8 ctivity (oral excitatory and anal inhibitory junction potentials) and Ca(2+) waves in LM and CM.
9         Responses to beta-NAD and inhibitory junction potentials are blocked by the P2Y1-selective an
10 junction, and the current-voltage curves and junction potentials are strongly and self-consistently m
11 servations cannot be explained by the liquid junction potential between two mutually miscible electro
12 rfacial potential with an additive diffusion/junction potential due to the increase in ionization fro
13 represents a discreet cholinergic excitatory junction potential (EJP) that involves the synaptic acti
14                        (5) Evoked excitatory junction potentials (EJP) were partially blocked by 4-DA
15 e cells to examine excitatory and inhibitory junction potentials (EJPs and IJPs).
16  microm), an ongoing discharge of excitatory junction potentials (EJPs) and inhibitory junction poten
17 ns evoked an ongoing discharge of excitatory junction potentials (EJPs) at the oral recording site (r
18 T potently facilitated B38-evoked excitatory junction potentials (EJPs) but had only a small effect o
19 CgTX GVIA) irreversibly abolished excitatory junction potentials (EJPs) evoked by trains of < or = fi
20 ormed intracellular recordings of excitatory junction potentials (EJPs) in the muscle fibers to deter
21 tion potentials (IJPs) anally, or excitatory junction potentials (EJPs) orally.
22 ding electrodes elicited compound excitatory junction potentials (EJPs) synchronously in both muscles
23       Supramaximal stimuli evoked excitatory junction potentials (EJPs) which could be divided into t
24  time-locked with the onset of an inhibitory junction potential (IJP) at an anal recording electrode,
25                                   Inhibitory junction potentials (IJP) of circular smooth muscle of g
26 ls showed an ongoing discharge of inhibitory junction potentials (IJPs) anally, or excitatory junctio
27                                   Inhibitory junction potentials (IJPs) and relaxations evoked in res
28 bitory nerve stimulation elicited inhibitory junction potentials (IJPs) and relaxations in wild-type
29 ssion resulting in a reduction in inhibitory junction potentials (IJPs) in colonic circular muscle.
30 eld stimulation evoked purinergic inhibitory junction potentials (IJPs) in CSMCs.
31 of OFQ on muscle contractions and inhibitory junction potentials (IJPs) in rat colon.
32                        EVS evoked inhibitory junction potentials (IJPs) in wild type muscles that wer
33 in PDGFRalpha(+) cells by EFS and inhibitory junction potentials (IJPs) recorded with intracellular m
34 between colonic MMCs, spontaneous inhibitory junction potentials (IJPs) were always present.
35 ry junction potentials (EJPs) and inhibitory junction potentials (IJPs) were recorded simultaneously
36 sed in relation to the idea that spontaneous junction potentials in colonic CM are not monoquantal ev
37 y of membrane potential following inhibitory junction potentials in gastrointestinal smooth muscle or
38  ongoing oral excitatory and anal inhibitory junction potentials in the CM.
39 al field stimulation yielded fast excitatory junction potentials in the smooth muscle that were block
40 ngs from CM cells revealed either no ongoing junction potentials, or alternatively, small potentials
41 The amplitude of NO-mediated slow inhibitory junction potentials (S-IJPs) evoked by electric field st
42                       Spontaneous excitatory junction potentials (SEJPs) were also recorded from most
43 y junction potentials (sIJPs) and excitatory junction potentials (sEJPs) were recorded from all anima
44 gesting that they are spontaneous excitatory junction potentials (sEJPs).
45                       Spontaneous inhibitory junction potentials (sIJPs) and excitatory junction pote
46 ime with those in CM, spontaneous inhibitory junction potentials (sIJPs) were found to occur synchron
47 region of smooth muscle at which spontaneous junction potentials (sJPs) were coordinated in both spac
48 reduction in evoked and miniature excitatory junction potentials, suggesting a neuronal deficit.
49 nt for salinity-induced variations in liquid junction potentials that, if not taken into account, wou
50  light resulted in excitatory and inhibitory junction potentials, the electrical events underlying co
51                                   The liquid junction potentials were estimated in the framework of I
52 Slow wave amplitude and nitrergic inhibitory junction potentials were reduced while solid emptying wa

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